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01 5Alvogen
02 2Amneal Pharmaceuticals
03 1Ascent Innovative Medicines
04 1Bausch & Lomb Incorporated
05 1Bioglan AB
06 2Chartwell Pharmaceuticals llc
07 4Cosette Pharma
08 2Encube Ethicals
09 1FARMA 1 Srl
10 6Fougera Pharmaceuticals Inc.
11 1Glenmark Pharmaceuticals
12 1Macleods Pharmaceuticals Limited
13 1Novel Laboratories, Inc.
14 2PAI Pharmaceutical Associates
15 2Padagis
16 1Perrigo Company plc
17 1Pharmaceutical Annotations, Sl
18 1Quagen Pharma
19 1SUN PHARMA CANADA
20 1ScieGen Pharmaceuticals
21 3TEOFARMA Srl
22 11Taro Pharmaceutical Industries
23 5Teofarma
24 5Teva Pharmaceutical Industries
25 1Xiromed
26 1Zydus Lifesciences
27 1Zydus Pharmaceuticals
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01 2CREAM
02 22CREAM;TOPICAL
03 5Cream
04 1Fluocinonide 0.05% 30Ml Lotion Dermatological Use
05 1GEL
06 5GEL;TOPICAL
07 1OINTMENT
08 7OINTMENT;TOPICAL
09 1Ointment
10 1Rectal Cream
11 14SOLUTION;TOPICAL
12 1Salve
13 3Blank
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01 3Allowed
02 3Authorized
03 18DISCN
04 4Prescription
05 30RX
06 6Blank
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01 1Abrasone
02 39FLUOCINONIDE
03 4FLUOCINONIDE EMULSIFIED BASE
04 1Flu 21
05 3LIDEX
06 1LIDEX-E
07 3LYDERM
08 1Metosyn
09 1Novoter
10 1Novoter Gentamicina
11 1TIAMOL CREAM 0.05%
12 1Topsym
13 2Topsym polyvalent
14 3Topsyn
15 1VANOS
16 1Blank
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01 4Canada
02 1India
03 4Italy
04 1Norway
05 3Spain
06 3Switzerland
07 48USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : LIDEX
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 16908
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : LIDEX-E
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 16908
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : LIDEX
Dosage Form : OINTMENT;TOPICAL
Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 16909
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLUOCINONIDE
Dosage Form : GEL;TOPICAL
Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 17373
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : LIDEX
Dosage Form : SOLUTION;TOPICAL
Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1984-04-06
Application Number : 18849
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VANOS
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.1%
Packaging :
Approval Date : 2005-02-11
Application Number : 21758
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLUOCINONIDE
Dosage Form : SOLUTION;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1988-12-02
Application Number : 71535
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLUOCINONIDE
Dosage Form : GEL;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1989-02-07
Application Number : 72537
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FLUOCINONIDE
Dosage Form : GEL;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1994-12-30
Application Number : 72933
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FLUOCINONIDE
Dosage Form : SOLUTION;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1995-02-27
Application Number : 72934
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FLUOCINONIDE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1994-10-17
Application Number : 73030
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLUOCINONIDE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1988-07-13
Application Number : 71790
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FLUOCINONIDE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1987-06-10
Application Number : 71500
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FLUOCINONIDE EMULSIFIED BASE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1989-01-19
Application Number : 72494
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLUOCINONIDE
Dosage Form : SOLUTION;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1989-08-02
Application Number : 72857
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FLUOCINONIDE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1989-02-06
Application Number : 72488
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : FLUOCINONIDE EMULSIFIED BASE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1989-02-07
Application Number : 72490
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLUOCINONIDE
Dosage Form : SOLUTION;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1989-02-07
Application Number : 72511
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLUOCINONIDE
Dosage Form : SOLUTION;TOPICAL
Dosage Strength : 0.05%
Packaging :
Approval Date : 1990-09-28
Application Number : 72522
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : FLUOCINONIDE
Dosage Form : CREAM;TOPICAL
Dosage Strength : 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1984-06-26
Application Number : 19117
Regulatory Info : DISCN
Registration Country : USA
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